Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19130 | A09 | 11643291 | C | T | missense_variant | MODERATE | c.178C>T|p.Pro60Ser |
S18 |
2 | BAA09g19130 | A09 | 11644172 | C | T | synonymous_variant | LOW | c.600C>T|p.Ile200Ile |
S263 |
3 | BAA09g19130 | A09 | 11644566 | G | A | missense_variant | MODERATE | c.994G>A|p.Asp332Asn |
S142 |
4 | BAA09g19130 | A09 | 11644760 | G | A | synonymous_variant | LOW | c.1188G>A|p.Val396Val |
S202 |
5 | BAA09g19130 | A09 | 11644768 | C | T | missense_variant | MODERATE | c.1196C>T|p.Ala399Val |
S18 |
6 | BAA09g19130 | A09 | 11647996 | C | T | downstream_gene_variant | MODIFIER | c.*2825C>T| |
S153 S157 S167 S236 S263 |
7 | BAA09g19130 | A09 | 11648256 | C | T | downstream_gene_variant | MODIFIER | c.*3085C>T| |
S18 |
8 | BAA09g19130 | A09 | 11648852 | C | T | downstream_gene_variant | MODIFIER | c.*3681C>T| |
S217 S248 |
9 | BAA09g19130 | A09 | 11649397 | G | A | downstream_gene_variant | MODIFIER | c.*4226G>A| |
S207 |